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Senior GCP QA Auditor – Full Time – Permanent – Remote – South America At Zigzag, you will become a pivotal member of our team, working alongside industry leading experts and delivering our client’s quality assurance
What the Associate II, Pharmacovigilance does at Worldwide Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific
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